HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 6-(4-Chlorophenyl)pyridine-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-(4-Chlorophenyl)pyridine-3-carbonitrile | HCID 14823234 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 6-(4-Chlorophenyl)pyridine-3-carboxamide | HCID 13502860 | — |
Reaction Steps
6-(4-Chlorophenyl)-3-pyridinecarbonitrile (1.61 grams), 30% hydrogen peroxide (3.0 cc.), 6 N sodium hydroxide (0.3 cc.), and about 6 ml ethanol were placed in a reaction vessel and cooled slightly. The reaction temperature rose to about 50° C. and the mixture was stirred for about 1 hour. After the reaction had cooled, a solid precipitate formed and was collected by filtration. As indicated by TLC, pure product was obtained by heating the solid in refluxing acetone, yield 0.4 gram, m.p. 245°-258° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04405552 |
| Source dataset | uspto-grants-1983_09 |
| ORD ID | ord-e25fa2f42b60444799cb2994e30568f8 |
| Source note | uspto-grants-1983_09 |